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Distribution and treatment of non alcoholic fatty liver disease in Indian people with diabetes and obesity related conditions

The Epidemiology and Treatment of Non-Alcoholic Fatty Liver Disease In Indian Population with Diabetes And Metabolic Syndrome.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2014/07/004725
Enrollment
100
Registered
2014-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Non Alcoholic Fatty Liver Disease

Interventions

Intervention1: Metformin,Metadoxine: 500 mg BD for 3 months Intervention2: Not Applicable: Not Applicable Control Intervention1: Not Applicable: Not Applicable

Sponsors

Osmania General Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with Type II Diabetes Mellitus and Metabolic Syndrome a. Fasting Blood Sugar >120 mg/dL b. Metabolic Syndrome diagnosed as per NCEP- ATP III criteria. 2. Patients with age >=18 years. 3. Patient with stable dose of diabetic medication for last three months. 4. Alcohol intake of

Exclusion criteria

Exclusion criteria: 1. Patient taking Thiazolidinedioneâ??s 2. Patients with cirrhosis. 3. Patients with NYHA class III-IV. 4. Patients having neurological disease. 5. Patient with uncontrolled blood pressure( 3 antihypertensive medication) 6. Patients on Drugs known to induce fatty liver such as methotrexate, estrogens, tamoxifen and amiodarone. 7. Unable to be followed for the duration of the clinical trial 8. Inability to obtain informed consent

Design outcomes

Primary

MeasureTime frame
a)To assess the prevalence and incidence of Non-Alcoholic Fatly Liver Disease (NAFLD) in patients with Diabetes and Metabolic Syndrome. b) Anthropometric measures.Timepoint: From enrollment

Secondary

MeasureTime frame
ALT alanine aminotransferase at the end of three months of treatment.Timepoint: From enrollment to 3 months;AST aspartate aminotransferase at the end of three months of treatment.Timepoint: from enrollment to 3 months

Countries

India

Contacts

Public ContactDr Rakesh Kumar Sahay

Osmania Medical College and Hospital

mohdalim786@yahoo.co.in

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026